ライフサイエンスコーパス: Lepidoptera

1 A and mE75B, were reported in Manduca sexta (Lepidoptera).

2 s, particularly as natural enemies of larval Lepidoptera.

3 llelochemicals and synthetic insecticides in Lepidoptera.

4 common in the Lycaenidae compared with other Lepidoptera.

5 males are primary endoparasitoids of eggs of Lepidoptera.

6 icantly from the mainly negative response of Lepidoptera.

7 f sex pheromone biosynthetic pathways in the Lepidoptera.

8 ecropin before the divergence of Diptera and Lepidoptera.

9 hanism to create structural color across the Lepidoptera.

10 mechanisms that are likely universal across lepidoptera.

11 e activation of induced responses to diverse Lepidoptera.

12 have evolved independently several times in Lepidoptera.

13 within the Nymphalidae in a phylogeny of the Lepidoptera.

14 genes related to locomotion and conserved in Lepidoptera.

15 from bacteria to the ancestors of ditrysian Lepidoptera.

16 to multiple cases of crypsis and mimicry in Lepidoptera.

17 and detoxification compared with specialist Lepidoptera.

18 y factor for the host's antiviral defense in Lepidoptera.

19 e of plant genera supporting the majority of Lepidoptera.

20 rred from bacteria to phytophagous mites and Lepidoptera.

21 ns Cry1Ab, Cry1Ac or both in four species of Lepidoptera.

22 erves as a resource for melanism research in Lepidoptera.

23 panded to the other insect groups except for Lepidoptera.

24 iation of moths and butterflies in the order Lepidoptera.

25 l, mechanism for diversification of tropical Lepidoptera.

26 y undescribed duplication of this gene among Lepidoptera.

27 orted as functional Cry1A toxin receptors in Lepidoptera.

28 ed to morphological diversity in Diptera and Lepidoptera.

29 cific biological example: oviposition in the Lepidoptera.

30 onspicuous feature of moths and butterflies (Lepidoptera),(1-3) their earliest evolution predates the

31 tly detected orders including Diptera (73%), Lepidoptera (65%), Trichoptera (38%), and Ephemeroptera

32 We show that, for boreal Lepidoptera, a combination of phenology and range shifts

33 nerating this diversity [9], particularly in Lepidoptera, a group with many species in decline [10, 1

34 olutionary evaluation of cycad-feeding among Lepidoptera along with a comprehensive review of their e

35 losely related taxa, such as Trichoptera and Lepidoptera (Amphiesmenoptera), differ greatly in sperm

36 Lepidoptera, an insect order of 150,000 species with div

37 ing of neuropeptidergic signaling systems in Lepidoptera and aid in the design of peptidomimetics, ps

38 p of forest canopy trees, emergence of adult Lepidoptera and arrival and subsequent breeding of migra

39 the differences in toxin specificity between Lepidoptera and Coleoptera insect orders.

40 thesis of volatile hydrocarbon pheromones of Lepidoptera and Coleoptera.

41 between the mode of action of Cry toxins in Lepidoptera and Coleoptera.

42 16.8% identity to trypsin genes of selected Lepidoptera and Diptera.

43 atest abundance at the ground level, whereas Lepidoptera and Hemiptera were more abundant in the uppe

44 s from 4 new orders (Orthoptera, Dermaptera, Lepidoptera and Opiliones) and 11 taxa (Acrididae, Gryll

45 h gaps that would be fruitfully addressed in Lepidoptera and other cycad-feeding insects.

46 al the constraints on genome architecture in Lepidoptera and provide a deeper understanding of chromo

47 erved in structures such as the proboscis of lepidoptera and snail shells or as vortices forming in f

48 suggest that this mechanism is common within Lepidoptera and that cortex has become a major target fo

49 the profound differences in responses of the Lepidoptera and the Diptera to juvenile hormone (JH).

50 and lim3 genes in wing pattern formation of Lepidoptera and the utility of museum-preserved collecti

51 ng the evolution of sexual dimorphism in the Lepidoptera, and alternative hypotheses have been neglec

52 ies (such as members of the hymenoptera, the lepidoptera, and amphibia) are highly mobile.

53 iensis convey toxicity to species within the Lepidoptera, and have wide potential applications in com

54 a, Isoptera, Hemiptera, Coleoptera, Diptera, Lepidoptera, and Hymenoptera), GABA-like immunoreactive

55 yx mori, highlighting its use as a model for Lepidoptera, and in sericulture and biotechnology.

56 Higher-level relationships within the Lepidoptera, and particularly within the species-rich su

57 In Lepidoptera, aposematic species typically harbour conspi

58 ural predator of eggs of Utetheisa ornatrix (Lepidoptera, Arctiidae), a moth that sequesters pyrroliz

59 In Utetheisa ornatrix (Lepidoptera, Arctiidae), the female mates preferentially

60 In the moth Utetheisa ornatrix (Lepidoptera: Arctiidae), females mate preferentially wit

61 the fall webworm, Hyphantria cunea (Drury) (Lepidoptera: Arctiidae), in China.

62 pest biologists and genome researchers, the Lepidoptera are an important insect group.

63 With over 1000 species already sequenced, Lepidoptera are at the forefront of biodiversity genomic

64 pheral nervous system and the wing scales of Lepidoptera are homologous structures.

65 Here we show that larval diets of tropical Lepidoptera are more specialized than those of their tem

66 Orthology properties suggest that the Lepidoptera are the fastest evolving insect order yet ex

67 The wing patterns of butterflies and moths (Lepidoptera) are diverse and striking examples of evolut

68 227 autosomes, exceptionally small even for Lepidoptera, are derived from extensive fragmentation of

69 taining Novartis event 176 on two species of Lepidoptera, black swallowtails and monarch butterflies,

70 repression is conserved between Diptera and Lepidoptera, but is absent in the Crustacea [6,7].

71 Lepidoptera (butterflies and moths) are one of the large

72 reference genomes of all ~11 000 species of Lepidoptera (butterflies and moths) found in Europe.

73 In Lepidoptera (butterflies and moths), the genomic region

74 assembly of CenH3-deficient kinetochores of Lepidoptera (butterflies and moths).

75 This study demonstrates that female Lepidoptera can synthesize a large fraction of egg amino

76 ary-specialist and dietary-generalist larval Lepidoptera (caterpillars) and their host plants in the

77 importance of resident microbiomes in larval Lepidoptera (caterpillars) is lacking, despite the fact

78 plete absence of female crossing-over in the Lepidoptera causes whole-chromosome hitchhiking of a sin

79 ing diverse insect orders including Diptera, Lepidoptera, Coleoptera, and Hymenoptera as well as in d

80 genetic analyses of Nymphalidae and of other Lepidoptera, combined with orthologue-level comparisons

81 Dispersal is important, and Lepidoptera communities appear to be highly dynamic acco

82 of the early-diverging lineages of ditrysian Lepidoptera, comprise about 1,800 species worldwide, inc

83 The wings of Lepidoptera contain a matrix of living cells whose funct

84 osed to stemborer Chilo partellus (Swinhoe) (Lepidoptera: Crambidae) eggs.

85 lex comprised of three lepidopteran species (Lepidoptera: Crambidae).

86 ecticidal activity against neonate larvae of Lepidoptera (Diatraea saccharalis), causing 60% mortalit

87 The largest four orders (Coleoptera, Lepidoptera, Diptera and Hymenoptera) represented 96.7%

88 structural database covering the Coleoptera, Lepidoptera, Diptera and Lepidoptera/Diptera specificity

89 ts caused by insect species in the orders of Lepidoptera, Diptera, and Coleoptera.

90 ncluding 39 viruses from hosts of the orders Lepidoptera, Diptera, and Hymenoptera, was reconstructed

91 ing the Coleoptera, Lepidoptera, Diptera and Lepidoptera/Diptera specificity classes.

92 ecific Cry3Aa, but most distantly related to Lepidoptera/Diptera-specific Cry2Aa.

93 similar responses of vegetation green-up and Lepidoptera emergence to temperature shifts support the

94 of pheromone structures used throughout the Lepidoptera, even among closely related species.

95 on of homeobox gene content across the order Lepidoptera, exemplifying the potential of newly generat

96 p represented in this study, the leaf-mining Lepidoptera, exhibits a wide range of subordinal taxonom

97 udies if new genomes, which cover additional Lepidoptera families are acquired.

98 larvae of many moths and butterflies (order: Lepidoptera) feed on cycads with apparent immunity.

99 tructures are used by moth species (Insecta: Lepidoptera) for long-distance mating signals.

100 In Lepidoptera, forewings and hindwings are mechanically co

101 tion of all homeobox genes in 123 species of Lepidoptera from 23 taxonomic families.

102 Interspecific analyses across four Lepidoptera further show that the relative size of senso

103 rimaea absoluta (Meyrick) (= Tuta absoluta) (Lepidoptera: Gelechiidae), is the most damaging insect p

104 The 865-Mb gypsy moth genome is the largest Lepidoptera genome sequenced to date and encodes ~13,300

105 family Lycaenidae and the largest available Lepidoptera genome.

106 composition of species-rich geometrid moth (Lepidoptera: Geometridae) assemblages in the mature temp

107 Two crucifer-specialist Lepidoptera had differing responses.

108 ies have reported that chromosome synteny in Lepidoptera has been well conserved, yet the number of h

109 Transposition of MINE-1 members in Lepidoptera has resulted in the disruption of (GAAA)(n)

110 We find most Lepidoptera have around 100 homeobox loci, including an

111 Lepidoptera have been characterized as lacking substanti

112 Most Lepidoptera have four Shx genes, divergent zen-derived l

113 The Lepidoptera have long been a favored model in evolutiona

114 igrants (15,000 t of biomass), predominantly Lepidoptera, Hemiptera, and Diptera, including many crop

115 stemin-mediated resistance to Manduca sexta (Lepidoptera) herbivory, demonstrating that MPK1 and MPK2

116 pical skipper butterfly Perichares philetes (Lepidoptera, Hesperiidae), described in 1775, which barc

117 ovarian cells of three different species of lepidoptera, i.e. B. mori (silkmoth), Samia cynthia rici

118 st an evolutionary split between Diptera and Lepidoptera in how the ecdysone biosynthetic pathway is

119 s by fluid-feeding insects in general and by Lepidoptera in particular.

120 ately promote the species diversification of Lepidoptera in temperate forests with respect to escape

121 istribution trends in 130 species of British Lepidoptera, in response to ~0.5 degrees C spring-temper

122 ura antennal unigenes had high homology with Lepidoptera insects, especially genes of the genus Spodo

123 (NomegaV), a T=4 icosahedral virus infecting Lepidoptera insects, were produced in insect cells using

124 host plant ranges and associated host plant-Lepidoptera interactions from across the contiguous Unit

125 od, the growth of the wing imaginal disks of Lepidoptera is dependent on continuous feeding.

126 Identification of Lepidoptera is normally based on the markings and morpho

127 Lepidoptera is the most herbivorous of all the insect or

128 biodiversification of butterflies and moths (Lepidoptera) is partly attributed to their unique mouthp

129 in the thoracic and subesophageal neurons of Lepidoptera larvae and may be absent in a subset of the

130 tation by inceptin, a peptide HAMP common in Lepidoptera larvae oral secretions.

131 Moths of genus Dendrolimus (Lepidoptera: Lasiocampidae) are among the major pests of

132 el genome assembly for Doratifera vulnerans (Lepidoptera: Limacodidae), which is venomous in the larv

133 n that populations of moths and butterflies (Lepidoptera) may be particularly susceptible to populati

134 In Lepidoptera, mir-193 is derived from a gigantic primary

135 Among the animals, the Lepidoptera (moths and butterflies) are second only to b

136 s by comparing host specialization in larval Lepidoptera (moths and butterflies) at eight different N

137 t specificity and beta diversity in tropical Lepidoptera (moths and butterflies) from New Guinea and

138 ewing), Hymenoptera (bees, ants, and wasps), Lepidoptera (moths), and Diptera (flies and mosquitoes).

139 eafhoppers, and bugs), Coleoptera (beetles), Lepidoptera (moths), and Hymenoptera (sawflies).(3)(,)(4

140 of the tobacco budworm, Heliothis virescens (Lepidoptera, Noctuidae).

141 Helicoverpa armigera Hubner (Lepidoptera: Noctuidae) is a devastating agricultural in

142 Smith) (Lepidoptera: Noctuidae) is a polyphagous pest indigenous

143 rol of noctuid pests, especially Spodoptera (Lepidoptera: Noctuidae) species.

144 ous insect herbivore, Spodoptera frugiperda (Lepidoptera: Noctuidae) through larval feeding assay.

145 ls on an agricultural pest, Trichoplusia ni (Lepidoptera: Noctuidae).

146 Fall armyworm (FAW) [Spodoptera frugiperda (Lepidoptera: Noctuidae)] on rice (Oryza sativa L.) using

147 act with female moths of the genus Gazalina (Lepidoptera, Notodontidae), or with their egg masses lai

148 the neotropical herbivore Anartia jatrophae (Lepidoptera: Nymphalidae).

149 The motif-patterns between Lepidoptera OBPs and CSPs are also compared.

150 Phylogenetic analysis of the Lepidoptera OBPs demonstrated that the OBP genes from th

151 to a phylogeny revealed two instances within Lepidoptera of convergently evolved L photopigment linea

152 er, representing lineages closely related to Lepidoptera: one represents the extinct Tarachoptera, wi

153 e dynamics of homeobox gene evolution across Lepidoptera or about how changes in homeobox gene number

154 tic XY system in Drosophila to ZW systems in Lepidoptera or mobile genes determining sex as found in

155 Unlike all other Lepidoptera OS examined, which preferentially contain in

156 How Lepidoptera overcome distance effects for gas transport

157 with conspicuous markings (Papilio troilus; Lepidoptera: Papilionidae), I tested the hypothesis that

158 val warning coloration in the genus Papilio (Lepidoptera: Papilionidae).

159 and carboxylesterases are involved in tuning Lepidoptera pheromones composition.

160 Cabbage White Butterfly [Pieris rapae (L.) (Lepidoptera: Pieridae)], which feeds on cruciferous host

161 in field populations of Plutella xylostella (Lepidoptera: Plutellidae).

162 redominantly midgut-expressed gene from many Lepidoptera possess key residues shown to be part of the

163 Prodoxus coloradensis (Lepidoptera: Prodoxidae) is a yucca moth, which feeds on

164 Mimicry and melanism in Lepidoptera provided the first convincing examples of na

165 The bagworm family (Lepidoptera: Psychidae) includes approximately 1000 spec

166 ionary distant species, Galleria mellonella (Lepidoptera: Pyralidae) and Anopheles gambiae (Diptera:

167 The mating system of Achroia grisella (Lepidoptera: Pyralidae) is characterized by male ultraso

168 ales of the lesser waxmoth Achroia grisella (Lepidoptera: Pyralidae) produce ultrasonic advertisement

169 lkworm, Antheraea pernyi (Guerin-Meneville) (Lepidoptera: Saturniidae), which is currently used.

170 erpillars of the silk moth genus Hyalophora (Lepidoptera; Saturniidae) construct multilayered cocoons

171 e to overlapping layers of scales and hairs (Lepidoptera, "scale wing").

172 Lepidoptera, similar to other insects, are believed to i

173 mitochondrial cytochrome c oxidase I from 28 Lepidoptera species and 1,359 individuals across four ho

174 shifts in northern range boundaries for 289 Lepidoptera species by using long-term data sampled over

175 t Survey shows that parasitism of particular Lepidoptera species is strongly host-plant-dependent, th

176 is structurally more closely similar to the Lepidoptera-specific Cry1Aa than the Coleoptera-specific

177 tagged databases have been used to discover Lepidoptera-specific genes, provide evidence for horizon

178 E75 activation by JH, in both Diptera and Lepidoptera, suggests a conserved function in the JH sig

179 rt on a previously undescribed mechanism for Lepidoptera that functions without a female-specific gen

180 timated there are over 100,000 moth species (Lepidoptera) that produce sex pheromones comprising comm

181 n ancestor of Tarachoptera, Trichoptera, and Lepidoptera; that Tarachoptera are monophyletic but thei

182 As with other Lepidoptera, the B. betularia W chromosome consists larg

183 ry selection of Vip3Aa-resistant colonies in Lepidoptera, the biochemical mechanisms underlying resis

184 Most Lepidoptera, the butterflies and moths, have 31 or 32 ch

185 Weight gain of two Lepidoptera, the generalist Trichoplusia ni and the facu

186 Until recently, deep-level phylogeny in Lepidoptera, the largest single radiation of plant-feedi

187 lved in numerous arthropod lineages, such as Lepidoptera, the moths and butterflies.

188 Given the importance of Lepidoptera to food webs and ecosystem function, efficie

189 tted fireworm moth, Choristoneura parallela (Lepidoptera: Tortricidae) were characterized and assayed

190 le Oriental fruit moths, Grapholita molesta (Lepidoptera: Tortricidae), to the aromatic plant volatil

191 CSD neurons were found in other Lepidoptera, Trichoptera, Diptera, Coleoptera, and Neuro

192 ostructures in neotropical mimetic clearwing Lepidoptera, using spectrophotometry and microscopy imag

193 ost use (i.e., parasitoid use of herbivorous Lepidoptera vs. pollinating Diptera) and functional grou

194 ifferentially expressed orthologous genes of Lepidoptera, we further found that holocentromere format

195 om Antiquan germ plasm that are resistant to Lepidoptera, we have demonstrated that a unique 33-kD cy

196 Although Coleoptera, Diptera, and Lepidoptera were the most consumed orders, we found that

197 y, alpha-amylases from Helicoverpa armigera (Lepidoptera) were not inhibited by AhAI while Tribolium

198 Geometrid moths (Lepidoptera) were the most important and consistent inse

199 cies on Earth are butterflies and moths, the Lepidoptera, which generally possess 31 chromosomes.

200 hiving of more than 150 studies of RNAi from Lepidoptera, which were previously unpublished.

201 Five species of Lepidoptera - White-headed prominent moth (Symmerista al

202 ld winters to be dominated by parasitoids of Lepidoptera, with the reverse being true for the parasit

203 Larvae of the genus Megalopyge (Lepidoptera: Zygaenoidea: Megalopygidae), known as asp o